Active Ingredient: LEVOBUNOLOL HYDROCHLORIDE
Proprietary Name: LEVOBUNOLOL HYDROCHLORIDE
Dosage Form; Route of Administration: SOLUTION/DROPS; OPHTHALMIC
Strength: 0.25%
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A074307
Product Number: 001
Approval Date: Mar 4, 1994
Applicant Holder Full Name: BAUSCH AND LOMB PHARMACEUTICALS INC
Marketing Status:
Discontinued
Patent and Exclusivity Information